KU Leuven Drug Delivery & Disposition , Gasthuisberg O&N2, Herestraat 49 Box 921, 3000 Leuven , Belgium.
KU Leuven Translational Research Center for Gastrointestinal Disorders (TARGID) , Gasthuisberg O&N1, Herestraat 49 Box 701, 3000 Leuven , Belgium.
Mol Pharm. 2019 Feb 4;16(2):573-582. doi: 10.1021/acs.molpharmaceut.8b00865. Epub 2019 Jan 9.
This study investigated gastrointestinal drug concentrations of the weakly acidic drug diclofenac when dosed to healthy volunteers after intake of the FDA standard meal. In gastrointestinal aspiration studies, postprandial conditions are usually achieved using liquid or homogenized meals. However, these liquid meals may have a substantially different impact on the gastrointestinal physiology compared to a solid meal. To evaluate the effect of a solid meal on the gastrointestinal behavior of diclofenac, five healthy volunteers were recruited into a clinical study. Twenty minutes prior to diclofenac ingestion (Cataflam, 50 mg of potassium diclofenac), the volunteers were asked to eat a solid meal with the following composition corresponding to the FDA standard meal: 2 eggs, 2 bacon strips, 2 toasts, 4 ounces of hash brown potatoes, and 8 ounces of milk. Gastric and duodenal fluids were collected as a function of time, and blood samples were collected to link the gastrointestinal behavior to systemic exposure. In vivo observations were complemented with in vitro research to obtain a mechanistic understanding of diclofenac's intraluminal behavior. Ingestion of the solid meal resulted in intraluminal pH-profiles similar to earlier studies with a liquid meal. However, intraluminal drug disposition differed. In the stomach, a substantial fraction of diclofenac appeared dissolved, despite an unfavorable acidic pH. Successive in vitro tests suggested that the dissolution of diclofenac is higher in the complex gastric medium resulting from FDA standard meal ingestion compared to liquid meal ingestion. Despite the favorable pH and in contrast to a previous study with a liquid meal, significant amounts of non-dissolved diclofenac were observed in the intestine. Further in vitro tests revealed adsorption of dissolved diclofenac molecules to bacon fragments present in the FDA standard meal. This adsorption negatively affected the permeation of diclofenac across a physical barrier, suggesting that in vivo absorption is affected as well. Being the first time a gastrointestinal aspiration study is combined with the administration of a solid meal, the present study demonstrates that the intraluminal behavior of diclofenac (and possibly other drugs) heavily depends on the consistency and composition of the accompanied meal.
这项研究调查了在健康志愿者摄入 FDA 标准餐后,弱酸性药物双氯芬酸的胃肠道药物浓度。在胃肠道抽吸研究中,通常使用液体或匀浆餐来达到餐后状态。然而,与固体餐相比,这些液体餐可能对胃肠道生理学产生显著不同的影响。为了评估固体餐对双氯芬酸胃肠道行为的影响,招募了五名健康志愿者参加临床研究。在摄入双氯芬酸(Cataflam,50 毫克双氯芬酸钾)前 20 分钟,志愿者被要求吃一种与 FDA 标准餐相对应的固体餐,其组成如下:2 个鸡蛋、2 片培根、2 片面包、4 盎司土豆泥和 8 盎司牛奶。胃和十二指肠液被收集作为时间的函数,并采集血样将胃肠道行为与全身暴露联系起来。体内观察结果辅以体外研究,以获得双氯芬酸腔内行为的机制理解。固体餐的摄入导致腔内 pH 曲线与先前使用液体餐的研究相似。然而,腔内药物处置不同。在胃中,尽管 pH 值不利,但双氯芬酸的很大一部分似乎溶解。连续的体外测试表明,与摄入液体餐后相比,在源自 FDA 标准餐后摄入的复杂胃介质中,双氯芬酸的溶解程度更高。尽管 pH 值有利,但与之前使用液体餐后的研究相反,在肠道中观察到大量未溶解的双氯芬酸。进一步的体外测试表明,溶解的双氯芬酸分子被 FDA 标准餐中存在的培根碎片吸附。这种吸附会对双氯芬酸穿过物理屏障的渗透产生负面影响,表明体内吸收也会受到影响。作为首次将胃肠道抽吸研究与固体餐给药相结合的研究,本研究表明,双氯芬酸(和可能其他药物)的腔内行为在很大程度上取决于伴随餐的一致性和组成。